tissue culture cells 中文意思是什麼
tissue culture cells
解釋
組織培養細胞-
Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel
結果如下：皮下包埋卜周者，無細胞真皮基質漸與周圍組織粘附，顏色由蒼白轉紅；皮下包埋3周者，無細胞真皮基質與周圍組織緊密枯附，盾晰葉辯；術后卜周，包埋的基質面積變化較包埋前無統計學差異o川0引，術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ） 。光鏡下術后卜周，宿主的淋巳組織細胞、成纖維細胞浸入生長，釉附在膠原纖維上，少量血管內皮細胞浸入基質；術后34周，無細胞真皮基質內較多的血管形成，故可認為無細胞真皮基質免疫原性低，能誘導宿主的成纖維細胞、巨噬細胞浸入生長，為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究， sd大鼠10隻，在其背部卜方造成全厚皮膚缺損的創面 -
For the cryogenic preservation of fish, in this paper we made the primary culture of the kidney of allotetroploid crucian carp and primary studies were carried out on cryopreservation culture offish embryo cells derived from misgurnus auguillicaudatus or grass carp, the results of the experiments are as follows : the primary cell culture of the kidney tissue derived from allotetroploid crucian carp was carried out using tissue adherent culture, the primary observations of the growth conditions and morphology of the primary culture and subculture cells which originally come from the kidney tissue were also made
本文主要從魚類種質保存的目的出發，一方面以四倍體鯽鯉魚為材料，對四倍體鯽鯉魚腎臟組織進行初步培養，為建立相應細胞庫及下一步培養凍存的魚類胚胎細胞奠定基礎；另一方面，以魚類組織細胞培養技術為基礎，泥鰍胚胎細胞為材料，對魚類胚胎細胞凍存培養方法進行初步研究，並應用該技術方法對草魚早期胚胎細胞進行凍存培養實驗。報告如下：本文用組織貼壁法對四倍體鯽鯉魚腎組織進行原代、傳代培養。 -
The results as follows : 1 ) the primary culture of qinchuan - scalper skin cells could be derived by fragment of tissue dispersed and cold digested single cell, collegenase i ( 150iu ml - 1 " ) and trypsin ( 0. 05 % ) being used at the same time is best to dissociate qinchuan - scalper skin tissue, which is appropriate to obtain qinchuan - scalper skin cells
組織塊法、分散單細胞及dispase冷消化法單細胞均能獲得好的秦川牛皮膚組織原代培養物。其中150iu ? ml ~ （ - 1 ）膠原酶i與0 . 05胰蛋白酶（ 1 ： 1 ）同時應用能更好的分離秦川牛皮膚組織，是獲得秦川牛皮膚細胞的適宜方法。 -
In terms with the principle of fusarium oxysporiun caused plant disease : bundles were blocked and fusarid acid killing cells was formed by hyphae so that caused water metabolism abnormal and plant wilting. in order to find out effective method of anti - fiisarium oxysporuin, long ya lillium was taken as material with plant tissue culture and genetic transformation techniques in this paper
針對尖孢鐮刀菌的致病機理：菌絲阻塞維管束引起水分代謝失常和菌絲在植物體內產生毒素（鐮刀菌酸）損害膜結構造成代謝失常，從而導致植物萎焉。本實驗以龍牙百合為研究對象，應用細胞工程中的離體培養方法並結合轉基因技術，以期找到抗尖孢鐮刀菌的有效途徑。 -
Isolation, culture and identification of human adipose tissue derived stem cells
人脂肪組織分離培養基質幹細胞的方法及其表型鑒定 -
Figure 2. b, on high - power magnification microscopy, the specimen showed a patternless tissue culture - like appearance with multiple mitoses and extraasated red blood cells
圖2b ，高倍顯微鏡檢查，標本顯示無圖案的「組織培養樣」表現，伴有大量有絲分裂和紅細胞外滲。 -
Conclusion this is a serum - free culture system for developing a conjunctival epithelial explants with improved purify and proliferative, which are important for the basic research and tissue engineer of conjunctival epithelial cells
結論無血清培養系統的組織塊培養法可為結膜上皮細胞的疾病、藥理毒理研究及培養移植的結膜上皮細胞提供更為安全有效的細胞模型。 -
Seeding cells of vascnlar tissue engineering : mor phology and culture and proliferation of endothelial cell and smooth muscle cell obtained from an aorta
血管組織工程中單根主動脈培養的內皮細胞和平滑肌細胞形態學和生長增殖 -
Co 2 incubator is an advanced instrument for culture of cells, tissue and bacteria. it is a necessary key apparatus for making scientific researches in immunology, oncology, genetics and biological engineering. itis also widely applicable to the research and prosucon work in medical science, microbiology agricultural science and harmacology
Co 2培養箱是細胞.組織.細菌培養的一種先進儀器.是開展免疫學.腫瘤學.遺傳學.及生物工程所必須的關鍵設備，廣泛應用於醫學.微生物.農業科學藥物學的研究和生產 -
With the advancement of tissue cytobiology and material engineering, by the way of tissue engineering, it is compatibile that we are going to culture the smg. the principle of the construction of tissue engineering smg is that the smg cells are isolated and cultured in vitro, and the seeded cells in the three - dimensional scaffolds
組織工程學研究的進展，無疑給解決這一問題帶來新的希望，隨著細胞生物學和材料工程學的發展，應用組織工程學的方法，在體外培養有生物活性，且在結構和功能上與自體頜下腺相類似的組織工程化頜下腺成為可能。 -
In an attempt to create a novel, entirely autologous tissue - engineered adipose substitute, we extracted human stromal cells from either lipoaspirated or resected fat, and assessed their capacity to produce a three - dimensional adipose tissue using an adapted “ self - assembly ” culture methodology
為了構建一種全新的完全自體的組織工程脂肪的替代物，我們從吸脂術或切割的脂肪中提取間質細胞，採用自組裝培養方法分析他們構建三維脂肪組織的能力。 -
Culture a population of microorganisms or dissociated cells of a tissue grown on or within a solid or liquid medium for experimental purposes
培養：以試驗為目的在固體或液體培養基上生長的微生物種群或解離的細胞或組織。
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